Micromolding of shape-controlled, harvestable cell-laden hydrogels

被引:263
作者
Yeh, Judy
Ling, Yibo
Karp, Jeffrey M.
Gantz, Jay
Chandawarkar, Akash
Eng, George
Blumling, James, III
Langer, Robert
Khademhosseini, Ali [1 ]
机构
[1] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[2] MIT, Div Biol Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Elect Engn & Comp Sci, Cambridge, MA 02139 USA
[4] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[5] Franklin W Olin Coll Engn, Needham, MA 02492 USA
[6] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Ctr Biomed Engn, Boston, MA 02115 USA
关键词
microgels; tissue engineering; micromolding; biomaterials; cell encapsulation;
D O I
10.1016/j.biomaterials.2006.06.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Encapsulation of mammalian cells within hydrogels has great utility for a variety of applications ranging from tissue engineering to cell-based assays. In this work, we present a technique to encapsulate live cells in three-dimensional (3D) microscale hydrogels (microgels) of controlled shapes and sizes in the form of harvestable free standing units. Cells were suspended in methacrylated hyaluronic acid (MeHA) or poly(ethylene glycol) diacrylate (PEGDA) hydrogel precursor solution containing photoinitiator, micromolded using a hydrophilic poly(dimethylsiloxane) (PDMS) stamp, and crosslinked using ultraviolet (UV) radiation. By controlling the features on the PDMS stamp, the size and shape of the molded hydrogels were controlled. Cells within microgels were well distributed and remained viable. These shape-specific microgels could be easily retrieved, cultured and potentially assembled to generate structures with controlled spatial distribution of multiple cell types. Further development of this technique may lead to applications in 3D co-cultures for tissue/organ regeneration and cell-based assays in which it is important to mimic the architectural intricacies of physiological cell-cell interactions. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5391 / 5398
页数:8
相关论文
共 35 条
[1]   Fabrication of hyaluronic acid hydrogel beads for cell encapsulation [J].
Bae, KH ;
Yoon, JJ ;
Park, TG .
BIOTECHNOLOGY PROGRESS, 2006, 22 (01) :297-302
[2]   Probing heterotypic cell interactions: Hepatocyte function in microfabricated co-cultures [J].
Bhatia, SN ;
Balis, UJ ;
Yarmush, ML ;
Toner, M .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1998, 9 (11) :1137-1160
[3]   Controlled degradation and mechanical behavior of photopolymerized hyaluronic acid networks [J].
Burdick, JA ;
Chung, C ;
Jia, XQ ;
Randolph, MA ;
Langer, R .
BIOMACROMOLECULES, 2005, 6 (01) :386-391
[4]   Delivery of osteoinductive growth factors from degradable PEG hydrogels influences osteoblast differentiation and mineralization [J].
Burdick, JA ;
Mason, MN ;
Hinman, AD ;
Thorne, K ;
Anseth, KS .
JOURNAL OF CONTROLLED RELEASE, 2002, 83 (01) :53-63
[5]   A microfluidic biomaterial [J].
Cabodi, M ;
Choi, NW ;
Gleghorn, JP ;
Lee, CSD ;
Bonassar, LJ ;
Stroock, AD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (40) :13788-13789
[6]   In vitro and in vivo performance of porcine islets encapsulated in interfacially photopolymerized poly(ethylene glycol) diacrylate membranes [J].
Cruise, GM ;
Hegre, OD ;
Lamberti, FV ;
Hager, SR ;
Hill, R ;
Scharp, DS ;
Hubbell, JA .
CELL TRANSPLANTATION, 1999, 8 (03) :293-306
[7]   Efficiency of embryoid body formation and hematopoietic development from embryonic stem cells in different culture systems [J].
Dang, SM ;
Kyba, M ;
Perlingeiro, R ;
Daley, GQ ;
Zandstra, PW .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 78 (04) :442-453
[8]   Photoinitiated crosslinked degradable copolymer networks for tissue engineering applications [J].
Davis, KA ;
Burdick, JA ;
Anseth, KS .
BIOMATERIALS, 2003, 24 (14) :2485-2495
[9]  
Elisseeff J, 2000, J BIOMED MATER RES, V51, P164, DOI 10.1002/(SICI)1097-4636(200008)51:2<164::AID-JBM4>3.3.CO
[10]  
2-N